Illuminating devices with color stable thermoplastic light transmitting articles

ABSTRACT

Illuminating devices are disclosed having plastic light-transmitting article(s) formed from a thermoplastic composition including a polycarbonate having repeating structural carbonate units according to the formula: 
                         
in which at least 60 percent of the total number of R 1  groups contain aromatic moieties and the balance thereof are aliphatic, alicyclic, or aromatic. The composition also includes an epoxy additive having at least two epoxy groups per molecule and a phenolic diphosphite derived from pentaerythritol. The thermoplastic composition exhibits a dE (2000 hrs.) value of less than 1.5 after 2000 hours of heat aging at 130° C., measured according ISO 11664-4:2008(E)/CIE S 014-4/E:2007 using CIE illuminant D65 and a 2.5 mm thick molded plaque of the thermoplastic composition.

CROSS-REFERENCE TO RELATED APPLICATIONS

The present application is a Non-Provisional and claims the benefit of U.S. Provisional Application No. 61/828,413, filed on May 29, 2013, and also claims the benefit of U.S. Provisional Application No. 61/972,074, filed Mar. 28, 2014, the contents of which are incorporated herein in their entirety by reference.

BACKGROUND OF THE INVENTION

This disclosure relates to polycarbonate compositions and in particular to polycarbonate compositions having enhanced optical properties, methods of manufacture, and uses thereof.

Polycarbonates can provide a number of beneficial properties, and are used in the manufacture of articles and components for a wide range of applications, from automotive parts to electronic appliances. Polycarbonates, however, can undergo changes in their light absorbing and/or transmitting properties when they age, especially under the influence of heat and/or light exposure, resulting in reduced light transmission and/or color changes. Specifically, polycarbonates can develop a yellowish tint and become darker when processed into an article and when aged under the influence of heat and/or light.

There accordingly remains a need in the art for polycarbonate compositions that can provide desirable light absorbing and/or transmitting properties under various aging conditions, including polycarbonate compositions that have low yellowness and high light transmission when processed into an article (e.g. through injection molding) and when aged (e.g. at higher temperature or for a long time).

It is well known that certain additives can improve the color characteristics of virgin polycarbonate. Primary antioxidants such as hindered phenols can be added to polycarbonates to reduce discoloration of the formed articles during aging. These additives protect the material in the solid state against discoloration over time. Secondary antioxidants such as phosphites can protect the material during high temperature processing in the molten state such as with injection molding, leading to a better color of the formed article. These two types of antioxidants can be combined to optimize both the color of the article after formation as well as during its lifetime; however, this combination may not be effective to achieve desired discoloration performance in various applications such as long-pathlength lighting applications such as thick lenses, light guides etc. Although certain secondary antioxidants, e.g. those based on pentaerythriol, can be effective during molding, they reduce the longer term color stability and therefore cannot be added at high level.

Multifunctional epoxides can be used as additives for polymeric resins with the aim of increasing viscosity, improving hydrolytic stability and recyclability. However, for many polycarbonate compositions such as those having a free hydroxy content of greater than 150 ppm and/or prepared from a bisphenol having a sulfur content of greater than 2 ppm by weight, the epoxy additive can actually increase the yellowness of molded article.

EP 0 320 658 A1 indicates that a pentaerythrol based phosphite stabilizer is useful as a process stabilizer for polycarbonate compositions, but does not study the effect of (heat) aging. The patent indicates epoxy additives should not be added to the composition.

EP 0 885 929 A1 discloses compositions containing pentaerythrol based diphosphites and epoxy additives with the aim of improving processability, reducing splay and improving hydrolytic stability. No heat aging is investigated. BPA organic purity higher than 99.7% and/or restrictions to the hydroxyl content in the BPA used to make the polycarbonate are not being described.

U.S. Pat. No. 4,076,686 discloses polycarbonate compositions containing epoxy and phosphites indicating and advantage when replacing a dialkyl hydrogen phosphite partly with an epoxy additive. The advantage that is shown in color stability is small and appears to be due to the lowering of the phosphite level.

U.S. Pat. No. 7,297,381 discloses polycarbonate compositions containing epoxy and phosphite for light-diffusing films and articles. These materials contain light diffusing particles which render them unsuitable for use in lenses, light guides, display panels and other applications in which transparency is key.

US2013/0035441A1 discloses interfacially polymerized transparent polycarbonates where the polycarbonate has lower than 150 ppm hydroxyl groups and less than 2 ppm sulfur compounds with advantageous optical properties such as low starting color and good color stability in heat aging. US2013/0108820A1 discloses a process to make BPA and polycarbonate having a reduced sulfur content as well as containers made of such polycarbonate. Polycarbonates made according to these inventions exhibit improved color stability over other polycarbonates, but for long light path length applications or applications involving close proximity to light sources, further improvement is desired.

In spite of the advances described in the above references, there remains a need to achieve further improvements in starting color and color stability of polycarbonates for use in light-transmitting applications.

SUMMARY OF THE INVENTION

It has now been discovered that polycarbonate compositions as further described herein can provide enhanced optical qualities for light-transmitting articles in illuminating devices comprising a light source and the light-transmitting article.

In an embodiment, an illuminating device, comprises: a light source; and a light-transmitting article formed from a thermoplastic composition, positioned to provide a light transmission path from the light source through the light-transmitting article, with a distance, d, between the light source and the light-transmitting article of less than 40 mm, the light transmission path extending through the light-transmitting article and optionally through other light-transmitting article(s) comprising the thermoplastic composition such that the total distance, p, of the light transmission path through the light-transmitting article is at least 3 mm; wherein the thermoplastic composition comprises a polycarbonate having repeating structural carbonate units according to the formula

in which at least 60 percent of the total number of R¹ groups contain aromatic moieties and the balance thereof are aliphatic, alicyclic, or aromatic; the polycarbonate having been prepared through an interfacial polymerization process from BPA monomer having an organic purity higher than 99.70% by weight and having a hydroxyl content lower than 150 ppm by weight; 0.01 wt. % to 0.30 wt. %, based on the total weight of the thermoplastic composition, of an epoxy additive having at least two epoxy groups per molecule; and 0.01 wt. % to 0.30 wt. %, based on the total weight of the thermoplastic composition, of a phenolic diphosphite derived from pentaerythritol; wherein the thermoplastic composition has a sulfur content lower than 2 ppm, and wherein the thermoplastic composition exhibits a dE (2000 hrs.) value of less than 2.0 after 2000 hours of heat aging at 130° C., measured according ISO 11664-4:2008(E)/CIE S 014-4/E:2007 using CIE illuminant D65 and a 2.5 mm thick molded plaque of the thermoplastic composition.

In an embodiment, a method of using the device, comprises illuminating the light-transmitting article with the light source under conditions to subject the light-transmitting article to a temperature of 80° C. to 135° C.

In an embodiment, a method for making the illuminating device, comprises: disposing the light source the distance d of less than 40 mm from the light-transmitting plastic article such that the total distance, p, of the light transmission path is at least 3 mm.

The above described and other features are further described by the following figures and detailed description.

BRIEF DESCRIPTION OF THE DRAWINGS

The foregoing and other features, and advantages of the invention are described in the following detailed description taken in conjunction with the accompanying drawings in which:

FIG. 1 is a schematic depiction of an exemplary illuminating device as described herein;

FIG. 2A is a schematic depiction of another exemplary illuminating device as described herein;

FIG. 2B is an exploded view of a portion of the illuminating device of FIG. 2A illustrating the light guide surface comprising an embodiment of an optical grating structure; and

FIGS. 3 and 4 are plots of dE (2000 hrs.) values for test plaques of a thermoplastic composition described herein.

DETAILED DESCRIPTION OF THE INVENTION

Turning now to the Figures, FIG. 1 depicts an illuminating device 10 with a housing 12 (e.g., which can optionally comprising a reflective surface on its inner surface) around a light source 14 disposed therein. A light-transmitting article in the form of inner lens 16 is disposed at a distance, d, away from the light source. A second light-transmitting article in the form of outer lens 18 is disposed further away from the light source 14 than the inner lens 16. In operation, light (the paths of which are represented by arrowed dashed lines) is emitted from the light source 14 and travels through and is refracted by the inner lens 16 and the outer lens 18 where it is emitted from the illuminating device 10.

FIG. 2A depicts an illuminating device 20 with a housing 22 having a light source 24 disposed therein. A first light-transmitting article in the form of light guide 26 is disposed at a distance, d, from the light source 24. A second light-transmitting article in the form of lens 28 is disposed on one side of the light guide 26. In operation, light (the paths of which are represented by arrowed dashed lines) is emitted from the light source 24 and enters the light guide 26 through surface 30. The light guide is constructed and configured with the light source 24 such that the light's angle of incidence with respect to the normal axis of the smooth surfaces 32 and 34 is greater than the critical angle of the polycarbonate composition in the surrounding medium (e.g., air) so that light is internally reflected back into light guide 26 along the surfaces 32 and 34 as it promulgates through the light guide 26. Surface 39 can allow light to escape, or it can have a reflective coating to reflect light back into the interior of the light guide 26. At positions 36 and 38 along the light guide surface 32, the normally smooth surface 32 is instead configured with a sawtooth or other optical grating structure as shown in blowup view to the right. (See FIG. 2B) Internally propagating light impinging on the surface 32 at positions 36 and 38 is able to exit the light guide 26 from where it travels through the lens 28 where it is emitted from the illuminating device 20.

As mentioned above, the invention is directed to illuminating devices where the distance, d, between a light source and a light-transmitting article is less than 40 mm. However, the composition described herein also excels in more demanding environments where light-transmitting article is in even closer proximity to the light source. Accordingly, in some embodiments, the distance between the light source and the light-transmitting article is less than 20 mm. In some embodiments, the distance is less than 10 mm. In some embodiments, the distance is less than 5 mm. In some embodiments, d is effectively 0 where the light-transmitting article is in direct contact with the light source or a protective cover thereon.

As mentioned above, disclosed herein are illuminating devices (also referred to as a light-emitting device) where the light transmission path extending through the light-transmitting article and optionally through other light-transmitting article(s) comprising the polycarbonate composition such that the total distance, p, of the light transmission path through the light-transmitting article(s) is at least 3 mm. However, the composition described herein also excels in more demanding environments where even longer light-transmission paths through the light-transmitting article(s) are contemplated. Accordingly, in some embodiments, the light transmission path distance through the light-transmitting article(s) is at least 5 mm. In some embodiments, the light transmission path distance through the light transmitting article(s) is at least 7 mm. In some embodiments, the light transmission path distance through the light-transmitting article(s) is at least 10 mm. In some embodiments, the light transmission path distance through the light-transmitting article(s) is at least 20 mm.

Several representative light paths are indicated in FIGS. 1 and 2A using dotted lines. The light path, defined as the total linear distance through the material that light passes before leaving the object is indicated with p1 and p2 in FIG. 1, and with p3 and p4 in FIG. 2A. The total light path p is the sum of the light paths through individual components. Note that in the case of a light guide as shown in FIG. 2A, the path p4 can be shorter than the length of the guide (for light exiting the object earlier) but also longer than the length of the guide (through multiple internal reflections). Hence, light path p will be a distribution rather than a fixed number. As used herein, the length p of the light transmission path through the polycarbonate composition means the average of such distribution. The average light path length p can be readily calculated using known mathematical techniques by plotting the angle of incidence for all light exiting the illuminating device versus the light path length and then calculating an average of the distribution of light path lengths.

Of course, FIGS. 1 and 2A are exemplary in nature and are shown in relatively simple configurations to illustrate the principals involved. Practical designs for light-transmitting articles can have a higher complexity for applications such as an illuminant lens (e.g., a collimator lens), illuminant cover, a light guide (also known as an optical waveguide) (e.g., an optical fiber), an optical sheet (e.g., a transparent sheet, a display film, and so forth). The illuminating device which comprises the light-transmitting article can be any device that is lighted, such as a toy (e.g., a light sword, light saber, and so forth), an illuminant article of furniture (e.g., a lighted table, lighted chair, bar, etc. with light illuminating features therein), art object, a light (e.g., a lamp (e.g. motor vehicle headlamp, house lamp, security lamp, and so forth) and so forth. For example, the light-emitting device is a motor vehicle headlamp such as shown in FIGS. 1 and 2A. The light-transmitting article can be disposed within an internally reflective housing that directs light through a transparent front cover. Limited space requirements commonly found in automotive headlamps and other automotive lighting applications can necessitate configurations where the close-coupled light source and/or long light travel path benefits can be especially effective.

Illuminating devices using polycarbonate compositions described herein can be used in connection with other illuminating features of various materials such as multiple light sources, lenses, light guides, reflectors, covers and other light-modifying components. Lenses can be spherical or aspheric. Aspheric lenses can have significantly greater thickness variations than spherical lenses because the distance from the focal point to the lens edge is not constant as with a spherical lens, rendering aspheric lenses particularly susceptible to color variation or instability in the lens material. Accordingly, in some embodiments, the light-transmitting article is an aspheric lens.

The light source such as the light source 14, 24 in FIGS. 1 and 2A can be any type of light source. In some embodiments, the light source is an LED. Many LED's require a cover, lens, or other light-transmitting article in close proximity to the LED. Accordingly, in some embodiments, the light source is an LED disposed within any of the d distance values specified above with respect to the light-transmitting article (i.e., 20 mm, 10 mm, 5 mm or 0 mm). In some embodiments, the light source is a xenon arc or other light source of similar whiteness, where the optical properties and stability of the polycarbonates described are effectively utilized.

The polycarbonate used in the light-transmitting articles described herein has defined optical properties of a dE (2000 hrs.) value of less than 2.0, more specifically less than 1.5, and even more specifically less than 0.95 after 2000 hours of heat aging at 130° C., with the dE calculation based on a comparison between an un-aged sample and a sample subjected to 2000 hours of heat aging at 130° C., measured according ISO 11664-4:2008(E)/CIE S 014-4/E:2007 using CIE illuminant D65 and a 2.5 mm thick molded plaque of the thermoplastic composition. The color stability indicated by the above-described dE (2000 hrs.) values can be beneficial for compositions having an initial color that can be described by various CIELAB color space values, as specified by ISO 11664-4:2008(E)/CIE S 014-4/E:2007. With initial color, or starting color is meant the color of a molded plaque short after molding, before any aging (thermal, light) has taken place which might change the color of the plaque. In some exemplary embodiments, the thermoplastic exhibits CIELAB 1976 color space values of b*<0.56 and L*>95.65, measured according to ISO 11664-4:2008(E)/CIE S 014-4/E:2007 using CIE illuminant D65 and a 2.5 mm thick molded plaque of the thermoplastic composition. In some exemplary embodiments, the thermoplastic exhibits CIELAB 1976 color space values of b*<0.54 and L*>95.75, determined as described above. In some exemplary embodiments, the thermoplastic exhibits CIELAB 1976 color space values of b*<0.52 and L*>95.85, determined as described above. Unless otherwise specified, the dE (2000 hrs.) value and the CIELAB 1976 color space values, are all determined based on color measurements made using a Macbeth 7000A spectrophotometer with a D65 illuminant, 10° observer, in transmission mode, specular included, ultraviolet component excluded, and both lens and aperture set to large, where dE is calculated according to dE1976

As mentioned above, the thermoplastic composition includes a polycarbonate. A “polycarbonate” means compositions having repeating structural carbonate units of formula (1)

in which at least 60 percent of the total number of R¹ groups contain aromatic moieties and the balance thereof are aliphatic, alicyclic, or aromatic. The polycarbonate is prepared through an interfacial polymerization process from BPA monomer of an organic purity higher than 99.70% w and having a hydroxyl content lower than 150 ppm. In some embodiments, each R¹ is a C₆₋₃₀ aromatic group, that is, contains at least one aromatic moiety. R¹ can be derived from a dihydroxy compound of the formula HO—R¹—OH, in particular of formula (2) HO-A¹-Y¹-A²-OH  (2) wherein each of A¹ and A² is a monocyclic divalent aromatic group and Y¹ is a single bond or a bridging group having one or more atoms that separate A¹ from A². In some embodiments, one atom separates A¹ from A². Specifically, each R¹ can be derived from a dihydroxy aromatic compound of formula (3)

wherein R^(a) and R^(b) are each independently a halogen, C₁₋₁₂ alkoxy, or C₁₋₁₂ alkyl; and p and q are each independently integers of 0 to 4. It will be understood that R^(a) is hydrogen when p is 0, and likewise R^(b) is hydrogen when q is 0. Also in formula (3), X^(a) is a bridging group connecting the two hydroxy-substituted aromatic groups, where the bridging group and the hydroxy substituent of each C₆ arylene group are disposed ortho, meta, or para (specifically para) to each other on the C₆ arylene group. In some embodiments, the bridging group X^(a) is single bond, —O—, —S—, —S(O)—, —S(O)₂—, —C(O)—, or a C₁₋₁₈ organic group. The C₁₋₁₈ organic bridging group can be cyclic or acyclic, aromatic or non-aromatic, and can further comprise heteroatoms such as halogens, oxygen, nitrogen, sulfur, silicon, or phosphorous. The C₁₋₁₈ organic group can be disposed such that the C₆ arylene groups connected thereto are each connected to a common alkylidene carbon or to different carbons of the C₁₋₁₈ organic bridging group. In an embodiment, p and q is each 1, and R^(a) and R^(b) are each a C₁₋₃ alkyl group, specifically methyl, disposed meta to the hydroxy group on each arylene group.

In some embodiments, X^(a) is a substituted or unsubstituted C₃₋₁₈ cycloalkylidene, a C₁₋₂₅ alkylidene of formula —C(R^(c))(R^(d))— wherein R^(c) and R^(d) are each independently hydrogen, C₁₋₁₂ alkyl, C₁₋₁₂ cycloalkyl, C₇₋₁₂ arylalkyl, C₁₋₁₂ heteroalkyl, or cyclic C₇₋₁₂ heteroarylalkyl, or a group of the formula —C(═R^(e))— wherein R^(e) is a divalent C₁₋₁₂ hydrocarbon group. Groups of this type include methylene, cyclohexylmethylene, ethylidene, neopentylidene, and isopropylidene, as well as 2-[2.2.1]-bicycloheptylidene, cyclohexylidene, cyclopentylidene, cyclododecylidene, and adamantylidene.

In some embodiments, X^(a) can be a C₁₋₁₈ alkylene group, a C₃₋₁₈ cycloalkylene group, a fused C₆₋₁₈ cycloalkylene group, or a group of the formula —B¹-G-B²— wherein B¹ and B² are the same or different C₁₋₆ alkylene group and G is a C₃₋₁₂ cycloalkylidene group or a C₆₋₁₆ arylene group. For example, X^(a) can be a substituted C₃₋₁₈ cycloalkylidene of formula (4)

wherein R^(r), R^(p), R^(q), and R^(t) are each independently hydrogen, halogen, oxygen, or C₁₋₁₂ hydrocarbon groups; Q is a direct bond, a carbon, or a divalent oxygen, sulfur, or —N(Z)— where Z is hydrogen, halogen, hydroxy, C₁₋₁₂ alkyl, C₁₋₁₂ alkoxy, or C₁₋₁₂ acyl; r is 0 to 2, t is 1 or 2, q is 0 or 1, and k is 0 to 3, with the proviso that at least two of R^(r), R^(p), R^(q), and R^(t) taken together are a fused cycloaliphatic, aromatic, or heteroaromatic ring. It will be understood that where the fused ring is aromatic, the ring as shown in formula (4) will have an unsaturated carbon-carbon linkage where the ring is fused. When k is one and i is 0, the ring as shown in formula (4) contains 4 carbon atoms, when k is 2, the ring as shown in formula (4) contains 5 carbon atoms, and when k is 3, the ring contains 6 carbon atoms. In an embodiment, two adjacent groups (e.g., R^(q) and R^(t) taken together) form an aromatic group, and in another embodiment, R^(q) and R^(t) taken together form one aromatic group and R^(r) and R^(p) taken together form a second aromatic group. When R^(q) and R^(t) taken together form an aromatic group, R^(p) can be a double-bonded oxygen atom, i.e., a ketone.

Bisphenols (4) can be used in the manufacture of polycarbonates containing phthalimidine carbonate units of formula (4a)

wherein R^(a), R^(b), p, and q are as in formula (4), R³ is each independently a C₁₋₆ alkyl group, j is 0 to 4, and R₄ is a C₁₋₆ alkyl, phenyl, or phenyl substituted with up to five C₁₋₆ alkyl groups. In particular, the phthalimidine carbonate units are of formula (4b)

wherein R⁵ is hydrogen or a C₁₋₆ alkyl. In an embodiment, R⁵ is hydrogen. Carbonate units (4a) wherein R⁵ is hydrogen can be derived from 2-phenyl-3,3′-bis(4-hydroxy phenyl)phthalimidine (also known as N-phenyl phenolphthalein bisphenol, or “PPPBP”) (also known as 3,3-bis(4-hydroxyphenyl)-2-phenylisoindolin-1-one).

Other bisphenol carbonate repeating units of this type are the isatin-derived carbonate units of formula (4c) and (4d)

wherein R^(a) and R^(b) are each independently C₁₋₁₂ alkyl, p and q are each independently 0 to 4, and R^(i) is C₁₋₁₂ alkyl, phenyl, optionally substituted with 1 5 to C₁₋₁₀ alkyl, or benzyl optionally substituted with 1 to 5 C₁₋₁₀ alkyl. In an embodiment, R^(a) and R^(b) are each methyl, p and q are each independently 0 or 1, and R^(i) is C₁₋₄ alkyl or phenyl.

Examples of bisphenol carbonate units derived from bisphenols (4) wherein X^(a) is a substituted or unsubstituted C₃₋₁₈ cycloalkylidene include the cyclohexylidene-bridged, alkyl-substituted bisphenol of formula (4e)

wherein R^(a) and R^(b) are each independently C₁₋₁₂ alkyl, R^(g) is C₁₋₁₂ alkyl, p and q are each independently 0 to 4, and t is 0 to 10. In a specific embodiment, at least one of each of R^(a) and R^(b) are disposed meta to the cyclohexylidene bridging group. In an embodiment, R^(a) and R^(b) are each independently C₁₋₄ alkyl, R^(g) is C₁₋₄ alkyl, p and q are each 0 or 1, and t is 0 to 5. In another specific embodiment, R^(a), R^(b), and R^(g) are each methyl, r and s are each 0 or 1, and t is 0 or 3, specifically 0. For example,

Examples of other bisphenol carbonate units derived from bisphenol (4) wherein X^(a) is a substituted or unsubstituted C₃₋₁₈ cycloalkylidene include units (4f) (also known as adamantyl units) and units (4g)

wherein R^(a) and R^(b) are each independently C₁₋₁₂ alkyl, and p and q are each independently 1 to 4. In a specific embodiment, at least one of each of R^(a) and R^(b) are disposed meta to the cycloalkylidene bridging group. In an embodiment, R^(a) and R^(b) are each independently C₁₋₃ alkyl, and p and q are each 0 or 1. In another specific embodiment, R^(a), R^(b) are each methyl, p and q are each 0 or 1. Carbonates containing units (4a) to (4g) are useful for making polycarbonates with high glass transition temperatures (Tg) and high heat distortion temperatures.

Other useful aromatic dihydroxy compounds of the formula HO—R¹—OH include compounds of formula (6)

wherein each R^(h) is independently a halogen atom, a C₁₋₁₀ hydrocarbyl such as a C₁₋₁₀ alkyl group, a halogen-substituted C₁₋₁₀ alkyl group, a C₆₋₁₀ aryl group, or a halogen-substituted C₆₋₁₀ aryl group, and n is 0 to 4. The halogen is usually bromine.

Some illustrative examples of specific aromatic dihydroxy compounds include the following: 4,4′-dihydroxybiphenyl, 1,6-dihydroxynaphthalene, 2,6-dihydroxynaphthalene, bis(4-hydroxyphenyl)methane, bis(4-hydroxyphenyl)diphenylmethane, bis(4-hydroxyphenyl)-1-naphthylmethane, 1,2-bis(4-hydroxyphenyl)ethane, 1,1-bis(4-hydroxyphenyl)-1-phenylethane, 2-(4-hydroxyphenyl)-2-(3-hydroxyphenyl)propane, bis(4-hydroxyphenyl)phenylmethane, 2,2-bis(4-hydroxy-3-bromophenyl)propane, 1,1-bis(hydroxyphenyl)cyclopentane, 1,1-bis(4-hydroxyphenyl)cyclohexane, 1,1-bis(4-hydroxyphenyl)isobutene, 1,1-bis(4-hydroxyphenyl)cyclododecane, trans-2,3-bis(4-hydroxyphenyl)-2-butene, 2,2-bis(4-hydroxyphenyl)adamantane, alpha, alpha′-bis(4-hydroxyphenyl)toluene, bis(4-hydroxyphenyl)acetonitrile, 2,2-bis(3-methyl-4-hydroxyphenyl)propane, 2,2-bis(3-ethyl-4-hydroxyphenyl)propane, 2,2-bis(3-n-propyl-4-hydroxyphenyl)propane, 2,2-bis(3-isopropyl-4-hydroxyphenyl)propane, 2,2-bis(3-sec-butyl-4-hydroxyphenyl)propane, 2,2-bis(3-t-butyl-4-hydroxyphenyl)propane, 2,2-bis(3-cyclohexyl-4-hydroxyphenyl)propane, 2,2-bis(3-allyl-4-hydroxyphenyl)propane, 2,2-bis(3-methoxy-4-hydroxyphenyl)propane, 2,2-bis(4-hydroxyphenyl)hexafluoropropane, 1,1-dichloro-2,2-bis(4-hydroxyphenyl)ethylene, 1,1-dibromo-2,2-bis(4-hydroxyphenyl)ethylene, 1,1-dichloro-2,2-bis(5-phenoxy-4-hydroxyphenyl)ethylene, 4,4′-dihydroxybenzophenone, 3,3-bis(4-hydroxyphenyl)-2-butanone, 1,6-bis(4-hydroxyphenyl)-1,6-hexanedione, ethylene glycol bis(4-hydroxyphenyl)ether, bis(4-hydroxyphenyl)ether, bis(4-hydroxyphenyl)sulfide, bis(4-hydroxyphenyl)sulfoxide, bis(4-hydroxyphenyl)sulfone, 9,9-bis(4-hydroxyphenyl)fluorine, 2,7-dihydroxypyrene, 6,6′-dihydroxy-3,3,3′,3′-tetramethylspiro(bis)indane (“spirobiindane bisphenol”), 3,3-bis(4-hydroxyphenyl)phthalimide, 2,6-dihydroxydibenzo-p-dioxin, 2,6-dihydroxythianthrene, 2,7-dihydroxyphenoxathin, 2,7-dihydroxy-9,10-dimethylphenazine, 3,6-dihydroxydibenzofuran, 3,6-dihydroxydibenzothiophene, and 2,7-dihydroxycarbazole, resorcinol, substituted resorcinol compounds such as 5-methyl resorcinol, 5-ethyl resorcinol, 5-propyl resorcinol, 5-butyl resorcinol, 5-t-butyl resorcinol, 5-phenyl resorcinol, 5-cumyl resorcinol, 2,4,5,6-tetrafluoro resorcinol, 2,4,5,6-tetrabromo resorcinol, or the like; catechol; hydroquinone; substituted hydroquinones such as 2-methyl hydroquinone, 2-ethyl hydroquinone, 2-propyl hydroquinone, 2-butyl hydroquinone, 2-t-butyl hydroquinone, 2-phenyl hydroquinone, 2-cumyl hydroquinone, 2,3,5,6-tetramethyl hydroquinone, 2,3,5,6-tetra-t-butyl hydroquinone, 2,3,5,6-tetrafluoro hydroquinone, 2,3,5,6-tetrabromo hydroquinone, or the like, or combinations comprising at least one of the foregoing dihydroxy compounds.

Specific examples of bisphenol compounds of formula (3) include 1,1-bis(4-hydroxyphenyl) methane, 1,1-bis(4-hydroxyphenyl) ethane, 2,2-bis(4-hydroxyphenyl) propane (hereinafter “bisphenol A” or “BPA”), 2,2-bis(4-hydroxyphenyl) butane, 2,2-bis(4-hydroxyphenyl) octane, 1,1-bis(4-hydroxyphenyl) propane, 1,1-bis(4-hydroxyphenyl) n-butane, 2,2-bis(4-hydroxy-2-methylphenyl) propane, 1,1-bis(4-hydroxy-t-butylphenyl) propane, 3,3-bis(4-hydroxyphenyl) phthalimidine, 2-phenyl-3,3-bis(4-hydroxyphenyl) phthalimidine (PPPBP), and 1,1-bis(4-hydroxy-3-methylphenyl)cyclohexane (DMBPC). Combinations comprising at least one of the foregoing dihydroxy compounds can also be used. In one specific embodiment, the polycarbonate is a linear homopolymer derived from bisphenol A, in which each of A¹ and A² is p-phenylene and Y¹ is isopropylidene in formula (3).

In some embodiments, the polycarbonate is derived from a bisphenol such as bisphenol A. For example, at least 90% of the R1 groups in formula (1) can be derived from a bisphenol such as bisphenol A. In some embodiments, all of the R1 groups are derived from a bisphenol such as bisphenol A. In more specific embodiments, the bisphenol has a sulfur content and/or a free hydroxyl group content as described in US 2013/0035441 A1 and US 2013/0108820 A1, the disclosures of which are incorporated herein by reference in their entirety. In some exemplary embodiments, the bisphenol has less than or equal to 150 ppm by weight free hydroxyl groups, based on the weight of the bisphenol. In some exemplary embodiments, the bisphenol comprises less than 2 ppm by weight sulfur, based on the weight of the bisphenol. In some exemplary embodiments the bisphenol comprises from greater than 0 to 2 ppm, e.g., 0.5 ppm to 2 ppm by weight sulfur, and in some exemplary embodiments the bisphenol comprises less than 0.5 ppm by weight sulfur, based on the weight of the bisphenol.

In some embodiments, the above-described bisphenol sulfur levels can be achieved using the melt crystal purification techniques described in the above-referenced US 2013/0108820A1. In some exemplary embodiments, a method of making a purified bisphenol comprises reacting phenol with acetone in the presence of a sulfur containing promoter to obtain a reaction mixture comprising a bisphenol such as bisphenol A, phenol, and the promoter, then cooling the reaction mixture to form a crystal stream comprising crystals of bisphenol and phenol and separating the crystals from the crystal stream. The separated crystals are then melted to form a molten stream of bisphenol, phenol, and sulfur; and this molten stream is contacted with a base to reduce a sulfur concentration in the molten stream and form a reduced sulfur stream. Phenol is then removed by desorption from this reduced sulfur stream, leaving a product stream of low sulfur-content bisphenol. In some exemplary embodiments, the promoter comprises a catalyst selected from 3-mercaptopropionic acid, methyl mercaptan, ethyl mercaptan, 2,2-bis(methylthio)propane, mercaptocarboxylic acid, and combinations comprising at least one of the foregoing promoters. In some exemplary embodiments, the promoter comprises 3-mercaptopropionic acid. In some exemplary embodiments, the base is an alkali solution. In some exemplary embodiments, the base is an anion exchange resin such as a tert-amine divinylbenzene/styrene ion exchange copolymer. In some exemplary embodiments, additional phenol is added to the molten stream prior to contacting the stream with a base.

In some embodiments, a high-purity bisphenol useful in preparing the polycarbonates used in the compositions described herein is prepared using an attached promoter ion exchange resin catalyst system, optionally in conjunction with a solvent crystallization step. The preparation of such high-purity bisphenols is described in US 2014/0051802A1 and US 2014/0051803A1, the disclosures of both of which are incorporated herein by reference in their entirety. In some exemplary embodiments, a bisphenol is prepared by contacting a phenol and at least one of a ketone, an aldehyde, or a combination thereof in the presence of an attached ion exchange resin catalyst comprising a dimethyl thiazolidine promoter, without utilizing a pretreatment and/or purification step for the phenol, ketone, and/or aldehyde. Solvent crystallization can be performed on reactor effluent from the above-described reaction after flashing off phenol from the reactor effluent.

“Polycarbonates” as used herein includes homopolycarbonates (wherein each R¹ in the polymer is the same), copolymers comprising different R¹ moieties in the carbonate (“copolycarbonates”), copolymers comprising carbonate units and other types of polymer units, such as ester units, and combinations comprising at least one of homopolycarbonates and/or copolycarbonates.

A specific type of copolymer is a polyester carbonate, also known as a polyester-polycarbonate. Such copolymers further contain, in addition to recurring carbonate chain units of formula (1), repeating units of formula (7)

wherein J is a divalent group derived from a dihydroxy compound, and can be, for example, a C₂₋₁₀ alkylene, a C₆₋₂₀ cycloalkylene a C₆₋₂₀ arylene, or a polyoxyalkylene group in which the alkylene groups contain 2 to 6 carbon atoms, specifically 2, 3, or 4 carbon atoms; and T is a divalent group derived from a dicarboxylic acid, and can be, for example, a C₂₋₁₀ alkylene, a C₆₋₂₀ cycloalkylene, or a C₆₋₂₀ arylene. Copolyesters containing a combination of different T and/or J groups can be used. The polyesters can be branched or linear. In another embodiment, J is a C₂₋₃₀ alkylene group having a straight chain, branched chain, or cyclic (including polycyclic) structure. J can be derived from an aromatic dihydroxy compound of formula (3) above, or from an aromatic dihydroxy compound of formula (4) above, or from an aromatic dihydroxy compound of formula (6) above.

Aromatic dicarboxylic acids that can be used to prepare the polyester units include isophthalic or terephthalic acid, 1,2-di(p-carboxyphenyl)ethane, 4,4′-dicarboxydiphenyl ether, 4,4′-bisbenzoic acid, or a combination comprising at least one of the foregoing acids. Acids containing fused rings can also be present, such as in 1,4-, 1,5-, or 2,6-naphthalenedicarboxylic acids. Specific dicarboxylic acids include terephthalic acid, isophthalic acid, naphthalene dicarboxylic acid, cyclohexane dicarboxylic acid, or a combination comprising at least one of the foregoing acids. A specific dicarboxylic acid comprises a combination of isophthalic acid and terephthalic acid wherein the weight ratio of isophthalic acid to terephthalic acid is 91:9 to 2:98. In another specific embodiment, J is a C₂₋₆ alkylene group and T is p-phenylene, m-phenylene, naphthalene, a divalent cycloaliphatic group, or a combination thereof. This class of polyester includes the poly(alkylene terephthalates).

The molar ratio of ester units to carbonate units in the copolymers can vary broadly, for example 1:99 to 99:1, specifically 10:90 to 90:10, more specifically 25:75 to 75:25, depending on the desired properties of the final composition.

In an embodiment, the polyester unit of a polyester-polycarbonate is derived from the reaction of a combination of isophthalic and terephthalic diacids (or derivatives thereof) with resorcinol. In another embodiment, the polyester unit of a polyester-polycarbonate is derived from the reaction of a combination of isophthalic acid and terephthalic acid with bisphenol A. In another embodiment, the polycarbonate units are derived from bisphenol A. In another embodiment, the polycarbonate units are derived from resorcinol and bisphenol A in a molar ratio of resorcinol carbonate units to bisphenol A carbonate units of 1:99 to 99:1.

The polycarbonates described herein are manufactured by interfacial polymerization. Although the reaction conditions for interfacial polymerization can vary, a process generally involves dissolving or dispersing a dihydric phenol reactant in aqueous caustic soda or potash, adding the resulting mixture to a water-immiscible solvent medium, and contacting the reactants with a carbonate precursor in the presence of a catalyst such as triethylamine and/or a phase transfer catalyst, under controlled pH conditions, e.g., 8 to 12. The most commonly used water immiscible solvents include methylene chloride, 1,2-dichloroethane, chlorobenzene, toluene, and the like.

Carbonate precursors include a carbonyl halide such as carbonyl bromide or carbonyl chloride, or a haloformate such as a bishaloformates of a dihydric phenol (e.g., the bischloroformates of bisphenol A, hydroquinone, or the like) or a glycol (e.g., the bishaloformate of ethylene glycol, neopentyl glycol, polyethylene glycol, or the like). Combinations comprising at least one of the foregoing types of carbonate precursors can also be used. Phosgene can also be a carbonate precursor in, an interfacial polymerization reaction to form carbonate linkages, which is referred to as a phosgenation reaction.

Among the phase transfer catalysts that can be used are catalysts of the formula (R³)₄Q⁺X, wherein each R³ is the same or different, and is a C₁₋₁₀ alkyl group; Q is a nitrogen or phosphorus atom; and X is a halogen atom or a C₁₋₈ alkoxy group or C₆₋₁₈ aryloxy group. phase transfer catalysts include, for example, [CH₃(CH₂)₃]₄NX, [CH₃(CH₂)₃]₄PX, [CH₃(CH₂)₅]₄NX, [CH₃(CH₂)₆]₄NX, [CH₃(CH₂)₄]₄NX, CH₃[CH₃(CH₂)₃]₃NX, and CH₃[CH₃(CH₂)₂]₃NX, wherein X is Cl⁻, Br⁻, a C₁₋₈ alkoxy group or a C₆₋₁₈ aryloxy group. A phase transfer catalyst can be used in an amount of 0.1 to 10 wt %, more specifically from 0.5 to 2 wt %, based on the weight of bisphenol in the polymerization reaction mixture.

All types of polycarbonate end groups are contemplated as being useful in the polycarbonate composition, provided that such end groups do not significantly adversely affect desired properties of the compositions.

Branched polycarbonate blocks can be prepared by adding a branching agent during polymerization. These branching agents include polyfunctional organic compounds containing at least three functional groups selected from hydroxyl, carboxyl, carboxylic anhydride, haloformyl, and mixtures of the foregoing functional groups. Specific examples include trimellitic acid, trimellitic anhydride, trimellitic trichloride, tris-p-hydroxy phenyl ethane, isatin-bis-phenol, tris-phenol TC (1,3,5-tris((p-hydroxyphenyl)isopropyl)benzene), tris-phenol PA (4(4(1,1-bis(p-hydroxyphenyl)-ethyl) alpha, alpha-dimethyl benzyl)phenol), 4-chloroformyl phthalic anhydride, trimesic acid, and benzophenone tetracarboxylic acid. The branching agents can be added at a level of 0.05 to 2.0 wt %, based on the total weight of the polymer. Mixtures comprising linear polycarbonates and branched polycarbonates can be used.

A chain stopper (also referred to as a capping agent) can be included during polymerization. The chain stopper limits molecular weight growth rate, and so controls molecular weight in the polycarbonate. Chain stoppers include certain mono-phenolic compounds, mono-carboxylic acid chlorides, and/or mono-chloroformates. Mono-phenolic chain stoppers are exemplified by monocyclic phenols such as phenol and C₁-C₂₂ alkyl-substituted phenols such as p-cumyl-phenol, resorcinol monobenzoate, and p- and tertiary-butyl phenol; and monoethers of diphenols, such as p-methoxyphenol. Alkyl-substituted phenols with branched chain alkyl substituents having 8 to 9 carbon atom can be specifically mentioned. Certain mono-phenolic UV absorbers can also be used as a capping agent, for example 4-substituted-2-hydroxybenzophenones and their derivatives, aryl salicylates, monoesters of diphenols such as resorcinol monobenzoate, 2-(2-hydroxyaryl)-benzotriazoles and their derivatives, 2-(2-hydroxyaryl)-1,3,5-triazines and their derivatives, and the like.

Mono-carboxylic acid chlorides can also be used as chain stoppers. These include monocyclic, mono-carboxylic acid chlorides such as benzoyl chloride, C₁-C₂₂ alkyl-substituted benzoyl chloride, toluoyl chloride, halogen-substituted benzoyl chloride, bromobenzoyl chloride, cinnamoyl chloride, 4-nadimidobenzoyl chloride, and combinations thereof; polycyclic, mono-carboxylic acid chlorides such as trimellitic anhydride chloride, and naphthoyl chloride; and combinations of monocyclic and polycyclic mono-carboxylic acid chlorides. Chlorides of aliphatic monocarboxylic acids with less than or equal to 22 carbon atoms are useful. Functionalized chlorides of aliphatic monocarboxylic acids, such as acryloyl chloride and methacryoyl chloride, are also useful. Also useful are mono-chloroformates including monocyclic, mono-chloroformates, such as phenyl chloroformate, alkyl-substituted phenyl chloroformate, p-cumyl phenyl chloroformate, toluene chloroformate, and combinations thereof.

Polyester-polycarbonates can be prepared by techniques and materials as described above for polycarbonates in general. Rather than utilizing the dicarboxylic acid or diol per se, the reactive derivatives of the acid or diol, such as the corresponding acid halides, in particular the acid dichlorides and the acid dibromides can be used. Thus, for example instead of using isophthalic acid, terephthalic acid, or a combination comprising at least one of the foregoing acids, isophthaloyl dichloride, terephthaloyl dichloride, or a combination comprising at least one of the foregoing dichlorides can be used.

As mentioned above, the thermoplastic composition also includes an epoxy additive having at least two epoxy groups per molecule. In some embodiments, the epoxy additive is an aliphatic epoxide having at least two epoxy groups per molecule and a molecular weight lower than 600 g/mol. Epoxy compounds useful as additives include epoxy modified acrylic oligomers or polymers (such as a styrene-acrylate-epoxy polymer, prepared from for example a combination of: a substituted or unsubstituted styrene such as styrene or 4-methylstyrene; an acrylate or methacrylate ester of a C₁₋₂₂ alkyl alcohol such as methyl acrylate, methyl methacrylate, ethyl acrylate, butyl acrylate, or the like; and an epoxy-functionalized acrylate such as glycidyl acrylate, glycidyl methacrylate, 2-(3,4-epoxycyclohexyl)ethyl acrylate, 2-(3,4-epoxycyclohexyl)ethyl methacrylate, or the like), or an epoxy carboxylate oligomer based on cycloaliphatic epoxides (such as, for example, 3,4-epoxycyclohexylmethyl-3,4-epoxycyclohexylcarboxylate, or the like).

The epoxy additive may comprise an additional functional group such as hydroxyl, carboxylic acid, carboxylic acid ester, and the like. More than one functional group may be present. Specific examples of the epoxy stabilizer include epoxidized soybean oil, epoxidized linseed oil, phenyl glycidyl ether, allyl glycidyl ether, tert-butylphenyl glycidyl ether, 3,4-epoxycyclohexylmethyl-3,4′-epoxy cyclohexyl carboxylate, 3,4-epoxy-6-methylcylohexylmethyl-3′,4′-epoxy-6′-methylcyclohexyl carboxylate, 2,3 epoxycyclohexylmethyl-3′,4′-epoxycyclohexyl carboxylate, 4-(3,4-epoxy-5-methylcyclohexyl)butyl-3′,4′-epoxycyclohexyl carboxylate, 3,4-epoxycyclohexylethyleneoxide, cyclohexylmethyl-3,4-epoxycyclohexyl carboxylate, 3,4 epoxy-6-methylcyclohexylmethyl-6′-methylcyclohexyl carboxylate, bisphenol A glycidyl ether, tetrabromobisphenol A glycidyl ether, diglycidyl phthalate, diglycidyl hexahydro phthalate, bis-epoxydicyclopentadienyl ether, bis-epoxyethylene glycol, bis-epoxycyclohexyl adipate, butadiene diepoxide, tetraphenylethylene epoxide, octyl epoxyphthalate, epoxidized polybutadiene, 3,4-dimethyl-1,2-epoxycyclo hexane, 3,5-dimethyl-1,2-epoxycyclohexane, 3-methyl-5 tert-butyl-1,2-epoxycyclohexane, octadecyl-2,2-dimethyl 3,4-epoxycyclohexyl carboxylate, N-butyl-2,2-dimethyl-3,4-epoxycyclohexyl carboxylate, cyclohexyl-2-methyl-3,4 epoxycyclohexyl carboxylate, N-butyl-2-isopropyl-3,4 epoxy-5-methylcyclohexyl carboxylate, octadecyl-3,4 epoxycyclohexyl carboxylate, 2-ethylhexyl-3′,4′ epoxycyclohexyl carboxylate, 4,6-dimethyl-2,3 epoxycyclohexyl-3′,4′-epoxycyclohexyl carboxylate, 4,5 epoxytetrahydrophthalic anhydride, 3-tert-butyl-4,5 epoxytetrahydrophthalic anhydride, diethyl-4,5-epoxy-cis 1,2-cyclohexyl dicarboxylate, and di-n-butyl-3-tert-butyl-4,5-epoxy-cis-1,2-cyclohexyl dicarboxylate. The epoxy compounds can be used singly or in combination. Of these, epoxy carboxylates such as alicyclic epoxy carboxylates (e.g., 3,4-epoxycyclohexylmethyl-3′,4′-epoxycyclo hexyl carboxylate) can be used.

In some embodiments, the epoxy additive is a carboxylate epoxy resin comprising a carboxylate diepoxide according to the formula:

Specific commercially available exemplary epoxy functionalized stabilizers include Cycloaliphatic Epoxide Resin ERL-4221 supplied by Union Carbide Corporation (a subsidiary of Dow Chemical), Danbury, Conn.; and epoxy functional acrylic (co)polymers such as JONCRYL™ ADR-4300 and JONCRYL™ ADR-4368, available from BASF Corporation, Sturtevant, Wis. Epoxy additives can be used in different amounts, for example from 0.01 to 0.25 wt. %, more specifically from 0.02 wt. % to 0.10 wt. %, based on the weight of the thermoplastic composition.

As mentioned above, the thermoplastic composition also includes a phenolic diphosphite derived from pentaerythritol. In some embodiments, the phenolic diphosphite is a compound according to the formula:

wherein R₁, R₂, R₃, R₄, R₅, R₆, R₇, R₈, R₉, and R₁₀ each independently represents hydrogen or a C₁₋₂₀ organic radical. In some embodiments, the position on the phenolic phenyl group to which the oxygen is attached is hindered, for example at the ortho and para positions. With respect to the above formula, for example, in some embodiments R₂, R₅, R₅, R₇, R₉, and R₁₀ are H and R₁, R₂, R₆, and R₈ each independently represents a C₁₋₂₀ organic radical, more specifically an alkaryl radical of 4 to 13 carbon atoms such as cumyl (e.g., bis(2,4-dicumyl)pentaerythritol diphosphite). Examples of phenolic diphosphites are disclosed in U.S. Pat. Nos. 5,364,895; 5,438,086; 6,613,823, the disclosures of which are incorporated herein by reference in their entirety. Phenolic diphosphates are also available commercially, e.g. under the Doverphos™ brand, e.g., Doverphos™ S-9228 and from ADK palmarole (e.g. ADK STAB PEP-36). The phenolic diphosphite can be present in the thermoplastic composition at different levels, for example, 0.02 wt. % to 0.30 wt. %, more specifically from 0.05 wt. % to 0.15 wt. %, based on the weight of the thermoplastic composition

The thermoplastic composition can further include additional additives as described below, with the proviso that the additive(s) are selected so as to not significantly adversely affect the desired properties of the thermoplastic composition, in particular the above-described optical properties. Such additives can be mixed at a suitable time during the mixing of the components for forming the composition. additives include reinforcing agents, antioxidants, heat stabilizers, light stabilizers (including ultraviolet (UV) light stabilizers), plasticizers, lubricants, mold release agents, antistatic agents, surface effect additives, radiation stabilizers, flame retardants, and anti-drip agents. Combinations of additives can also be used.

Antioxidant additives include additional organophosphites in addition to the phenolic diphosphite derived from pentaerythritol, such as tris(nonyl phenyl)phosphite, tris(2,4-di-t-butylphenyl)phosphite, distearyl pentaerythritol diphosphite; alkylated monophenols or polyphenols; alkylated reaction products of polyphenols with dienes, such as tetrakis[methylene(3,5-di-tert-butyl-4-hydroxyhydrocinnamate)]methane; butylated reaction products of para-cresol or dicyclopentadiene; alkylated hydroquinones; hydroxylated thiodiphenyl ethers; alkylidene-bisphenols; benzyl compounds; esters of beta-(3,5-di-tert-butyl-4-hydroxyphenyl)-propionic acid with monohydric or polyhydric alcohols; esters of beta-(5-tert-butyl-4-hydroxy-3-methylphenyl)-propionic acid with monohydric or polyhydric alcohols; esters of thioalkyl or thioaryl compounds such as distearylthiopropionate, dilaurylthiopropionate, ditridecylthiodipropionate, octadecyl-3-(3,5-di-tert-butyl-4-hydroxyphenyl)propionate, pentaerythrityl-tetrakis[3-(3,5-di-tert-butyl-4-hydroxyphenyl)propionate; amides of beta-(3,5-di-tert-butyl-4-hydroxyphenyl)-propionic acid, or combinations comprising at least one of the foregoing antioxidants. Antioxidants are used in amounts of 0.01 to 0.1 parts by weight, based on 100 parts by weight of the total composition.

Heat stabilizer additives include organophosphites such as triphenyl phosphite, tris-(2,6-dimethylphenyl)phosphite, tris-(mixed mono- and di-nonylphenyl)phosphite; phosphonates such as dimethylbenzene phosphonate, phosphates such as trimethyl phosphate, or combinations comprising at least one of the foregoing heat stabilizers. Heat stabilizers are used in amounts of 0.01 to 0.1 parts by weight, based on 100 parts by weight of the total composition.

Light stabilizers (including ultraviolet light (UV) absorbers) can also be used. Light stabilizers include benzotriazoles such as 2-(2-hydroxy-5-methylphenyl)benzotriazole and 2-(2-hydroxy-5-tert-octylphenyl)-benzotriazole, 2-hydroxy-4-n-octoxy benzophenone, or combinations comprising at least one of the foregoing light stabilizers. Light stabilizers are used in amounts of 0.01 to 5 parts by weight, based on 100 parts by weight of the total composition.

UV absorbers include hydroxybenzophenones; hydroxybenzotriazoles; hydroxybenzotriazines; cyanoacrylates; oxanilides; benzoxazinones; 2-(2H-benzotriazol-2-yl)-4-(1,1,3,3-tetramethylbutyl)-phenol (CYASORB™ 5411); 2-hydroxy-4-n-octyloxybenzophenone (CYASORB™ 531); 2-[4,6-bis(2,4-dimethylphenyl)-1,3,5-triazin-2-yl]-5-(octyloxy)-phenol (CYASORB™ 1164); 2,2′-(1,4-phenylene)bis(4H-3,1-benzoxazin-4-one) (CYASORB™ UV-3638); 1,3-bis[(2-cyano-3,3-diphenylacryloyl)oxy]-2,2-bis[[(2-cyano-3,3-diphenylacryloyl)oxy]methyl]propane (UVINUL* 3030); 2,2′-(1,4-phenylene)bis(4H-3,1-benzoxazin-4-one); 1,3-bis[(2-cyano-3,3-diphenylacryloyl)oxy]-2,2-bis[[(2-cyano-3,3-diphenylacryloyl)oxy]methyl]propane; phenol, 2-(2H-benzotriazol-2-yl)-4,6-bis(1-methyl-1-phenylethyl)-(TINUVIN™ 234); BCAP bismalonate from Clariant; nano-size inorganic materials such as titanium oxide, cerium oxide, and zinc oxide, all with particle size less than or equal to 100 nanometers; or combinations comprising at least one of the foregoing UV absorbers. UV absorbers are used in amounts of 0.01 to 5 parts by weight, based on 100 parts by weight of the total composition. Additives stabilizing against discoloration by gamma irradiation can also be used in the composition. Examples of such stabilizers are polyether polyols, polyether polyolesters, aromatic disulfides, hexylene glycol, poly(alkyleneglycol). Gamma stabilizing additives can be present in levels of 0.01 to 1.0 parts by weight, based on 100 parts by weight of the total composition.

Plasticizers, lubricants, and/or mold release agents can also be used. There is considerable overlap among these types of materials, which include phthalic acid esters such as dioctyl-4,5-epoxy-hexahydrophthalate; tris-(octoxycarbonylethyl)isocyanurate; tristearin; di- or polyfunctional aromatic phosphates such as resorcinol tetraphenyl diphosphate (RDP), the bis(diphenyl)phosphate of hydroquinone and the bis(diphenyl)phosphate of bisphenol A; poly-alpha-olefins; epoxidized soybean oil; silicones, including silicone oils; esters, for example, fatty acid esters such as alkyl stearyl esters, e.g., methyl stearate, stearyl stearate, pentaerythritol tetrastearate, and the like; combinations of methyl stearate and hydrophilic and hydrophobic nonionic surfactants comprising polyethylene glycol polymers, polypropylene glycol polymers, poly(ethylene glycol-co-propylene glycol) copolymers, or a combination comprising at least one of the foregoing glycol polymers, e.g., methyl stearate and polyethylene-polypropylene glycol copolymer in a solvent; waxes such as beeswax, montan wax, and paraffin wax. Such materials are used in amounts of 0.1 to 1 parts by weight, based on 100 parts by weight of the total composition.

Useful flame retardants include organic compounds that include phosphorus, bromine, and/or chlorine. Non-brominated and non-chlorinated phosphorus-containing flame retardants can be preferred in certain applications for regulatory reasons, for example organic phosphates and organic compounds containing phosphorus-nitrogen bonds.

Flame retardant aromatic phosphates include triphenyl phosphate, tricresyl phosphate, isopropylated triphenyl phosphate, phenyl bis(dodecyl)phosphate, phenyl bis(neopentyl)phosphate, phenyl bis(3,5,5′-trimethylhexyl)phosphate, ethyl diphenyl phosphate, 2-ethylhexyl di(p-tolyl)phosphate, bis(2-ethylhexyl) p-tolyl phosphate, tritolyl phosphate, bis(2-ethylhexyl) phenyl phosphate, tri(nonylphenyl)phosphate, bis(dodecyl) p-tolyl phosphate, dibutyl phenyl phosphate, 2-chloroethyl diphenyl phosphate, p-tolyl bis(2,5,5′-trimethylhexyl)phosphate, and 2-ethylhexyl diphenyl phosphate. Di- or polyfunctional aromatic phosphorus-containing compounds are also useful, for example resorcinol tetraphenyl diphosphate (RDP), the bis(diphenyl)phosphate of hydroquinone and the bis(diphenyl)phosphate of bisphenol A, respectively, and their oligomeric and polymeric counterparts. flame retardant compounds containing phosphorus-nitrogen bonds include phosphonitrilic chloride, phosphorus ester amides, phosphoric acid amides, phosphonic acid amides, phosphinic acid amides, and tris(aziridinyl)phosphine oxide. When used, phosphorus-containing flame retardants are present in amounts of 0.1 to 30 parts by weight, more specifically 1 to 20 parts by weight, based on 100 parts by weight of the total composition.

Halogenated materials can also be used as flame retardants, for example bisphenols of which the following are representative: 2,2-bis-(3,5-dichlorophenyl)-propane; bis-(2-chlorophenyl)-methane; bis(2,6-dibromophenyl)-methane; 1,1-bis-(4-iodophenyl)-ethane; 1,2-bis-(2,6-dichlorophenyl)-ethane; 1,1-bis-(2-chloro-4-iodophenyl)ethane; 1,1-bis-(2-chloro-4-methylphenyl)-ethane; 1,1-bis-(3,5-dichlorophenyl)-ethane; 2,2-bis-(3-phenyl-4-bromophenyl)-ethane; 2,6-bis-(4,6-dichloronaphthyl)-propane; and 2,2-bis-(3,5-dichloro-4-hydroxyphenyl)-propane 2,2 bis-(3-bromo-4-hydroxyphenyl)-propane. Other halogenated materials include 1,3-dichlorobenzene, 1,4-dibromobenzene, 1,3-dichloro-4-hydroxybenzene, and biphenyls such as 2,2′-dichlorobiphenyl, polybrominated 1,4-diphenoxybenzene, 2,4′-dibromobiphenyl, and 2,4′-dichlorobiphenyl as well as decabromo diphenyl oxide, as well as oligomeric and polymeric halogenated aromatic compounds, such as a copolycarbonate of bisphenol A and tetrabromobisphenol A and a carbonate precursor, e.g., phosgene. Metal synergists, e.g., antimony oxide, can also be used with the flame retardant. When present, halogen containing flame retardants are present in amounts of 1 to 25 parts by weight, more specifically 2 to 20 parts by weight, based on 100 parts by weight of the total composition. Alternatively, the thermoplastic composition can be essentially free of chlorine and bromine “Essentially free of chlorine and bromine” is defined as having a bromine and/or chlorine content of less than or equal to 100 parts per million by weight (ppm), less than or equal to 75 ppm, or less than or equal to 50 ppm, based on the total parts by weight of the composition.

Inorganic flame retardants can also be used, for example salts of C₁₋₁₆ alkyl sulfonate salts such as potassium perfluorobutane sulfonate (Rimar salt), potassium perfluoroctane sulfonate, tetraethylammonium perfluorohexane sulfonate, and potassium diphenylsulfone sulfonate; salts such as Na₂CO₃, K₂CO₃, MgCO₃, CaCO₃, and BaCO₃, or fluoro-anion complexes such as Li₃AlF₆, BaSiF₆, KBF₄, K₃AlF₆, KAlF₄, K₂SiF₆, and/or Na₃AlF₆. When present, inorganic flame retardant salts are present in amounts of 0.01 to 10 parts by weight, more specifically 0.02 to 1 parts by weight, based on 100 parts by weight of the total composition.

Tinting colorants can be added to the thermoplastic composition to achieve specifically targeted color space values, subject to compliance with L* specifications or other specifications described herein or elsewhere. Colorants include, for example, anthraquinones, perylenes, perinones, indanthrones, quinacridones, xanthenes, oxazines, oxazolines, thioxanthenes, indigoids, thioindigoids, naphtalimides, cyanines, xanthenes, methines, lactones, coumarins, bis-benzoxaxolylthiophenes (BBOT), napthalenetetracarboxylic derivatives, monoazo and disazo pigments, triarylmethanes, aminoketones, bis(styryl)biphenyl derivatives, and the like, as well as combinations comprising at least one of the foregoing colorants. The amount of colorant depends on the target color properties for the article, the spectral absorbance properties of the colorant(s), and the intrinsic color properties of the polycarbonate and any other materials or additives in the thermoplastic composition. The amount can vary, provided that it is kept below the level at which L* falls below target specifications, in some embodiments an L* value of 95.65, in some embodiments an L* value of 95.75, and in some embodiments an L* value of 98.85. Exemplary amounts can range from 0.00005 to 0.01 parts by weight per 100 parts by weight of polycarbonate resin.

Specific exemplary colorants include organic dyes such as coumarin 460 (blue), coumarin 6 (green), nile red or the like; lanthanide complexes; hydrocarbon and substituted hydrocarbon dyes; polycyclic aromatic hydrocarbons; scintillation dyes (preferably oxazoles and oxadiazoles); aryl- or heteroaryl-substituted poly(2-8 olefins); carbocyanine dyes; phthalocyanine dyes and pigments; oxazine dyes; carbostyryl dyes; porphyrin dyes; acridine dyes; anthraquinone dyes; arylmethane dyes; azo dyes; diazonium dyes; nitro dyes; quinone imine dyes; tetrazolium dyes; thiazole dyes; perylene dyes, perinone dyes; bis-benzoxazolylthiophene (BBOT); and xanthene dyes; fluorophores such as anti-stokes shift dyes which absorb in the near infrared wavelength and emit in the visible wavelength, or the like; luminescent dyes such as 5-amino-9-diethyliminobenzo(a)phenoxazonium perchlorate; 7-amino-4-methylcarbostyryl; 7-amino-4-methylcoumarin; 7-amino-4-trifluoromethylcoumarin; 3-(2′-benzimidazolyl)-7-N,N-diethylaminocoumarin; 3-(2′-benzothiazolyl)-7-diethylaminocoumarin; 2-(4-biphenylyl)-5-(4-t-butylphenyl)-1,3,4-oxadiazole; 2-(4-biphenylyl)-5-phenyl-1,3,4-oxadiazole; 2-(4-biphenyl)-6-phenylbenzoxazole-1,3; 2,5-Bis-(4-biphenylyl)-1,3,4-oxadiazole; 2,5-bis-(4-biphenylyl)-oxazole; 4,4′-bis-(2-butyloctyloxy)-p-quaterphenyl; p-bis(o-methylstyryl)-benzene; 5,9-diaminobenzo(a)phenoxazonium perchlorate; 4-dicyanomethylene-2-methyl-6-(p-dimethylaminostyryl)-4H-pyran; 1,1′-diethyl-2,2′-carbocyanine iodide; 1,1′-diethyl-4,4′-carbocyanine iodide; 3,3′-diethyl-4,4′,5,5′-dibenzothiatricarbocyanine iodide; 1,1′-diethyl-4,4′-dicarbocyanine iodide; 1,1′-diethyl-2,2′-dicarbocyanine iodide; 3,3′-diethyl-9,11-neopentylenethiatricarbocyanine iodide; 1,3′-diethyl-4,2′-quinolyloxacarbocyanine iodide; 1,3′-diethyl-4,2′-quinolylthiacarbocyanine iodide; 3-diethylamino-7-diethyliminophenoxazonium perchlorate; 7-diethylamino-4-methylcoumarin; 7-diethylamino-4-trifluoromethylcoumarin; 7-diethylaminocoumarin; 3,3′-diethyloxadicarbocyanine iodide; 3,3′-diethylthiacarbocyanine iodide; 3,3′-diethylthiadicarbocyanine iodide; 3,3′-diethylthiatricarbocyanine iodide; 4,6-dimethyl-7-ethylaminocoumarin; 2,2′-dimethyl-p-quaterphenyl; 2,2-dimethyl-p-terphenyl; 7-dimethylamino-1-methyl-4-methoxy-8-azaquinolone-2; 7-dimethylamino-4-methylquinolone-2; 7-dimethylamino-4-trifluoromethylcoumarin; 2-(4-(4-dimethylaminophenyl)-1,3-butadienyl)-3-ethylbenzothiazolium perchlorate; 2-(6-(p-dimethylaminophenyl)-2,4-neopentylene-1,3,5-hexatrienyl)-3-methylbenzothiazolium perchlorate; 2-(4-(p-dimethylaminophenyl)-1,3-butadienyl)-1,3,3-trimethyl-3H-indolium perchlorate; 3,3′-dimethyloxatricarbocyanine iodide; 2,5-diphenylfuran; 2,5-diphenyloxazole; 4,4′-diphenylstilbene; 1-ethyl-4-(4-(p-dimethylaminophenyl)-1,3-butadienyl)-pyridinium perchlorate; 1-ethyl-2-(4-(p-dimethylaminophenyl)-1,3-butadienyl)-pyridinium perchlorate; 1-Ethyl-4-(4-(p-dimethylaminophenyl)-1,3-butadienyl)-quinolium perchlorate; 3-ethylamino-7-ethylimino-2,8-dimethylphenoxazin-5-ium perchlorate; 9-ethylamino-5-ethylamino-10-methyl-5H-benzo(a) phenoxazonium perchlorate; 7-ethylamino-6-methyl-4-trifluoromethylcoumarin; 7-ethylamino-4-trifluoromethylcoumarin; 1,1′,3,3,3′,3′-hexamethyl-4,4′,5,5′-dibenzo-2,2′-indotricarboccyanine iodide; 1,1′,3,3,3′,3′-hexamethylindodicarbocyanine iodide; 1,1′,3,3,3′,3′-hexamethylindotricarbocyanine iodide; 2-methyl-5-t-butyl-p-quaterphenyl; N-methyl-4-trifluoromethylpiperidino-<3,2-g>coumarin; 3-(2′-N-methylbenzimidazolyl)-7-N,N-diethylaminocoumarin; 2-(1-naphthyl)-5-phenyloxazole; 2,2′-p-phenylen-bis(5-phenyloxazole); 3,5,3″″,5″″-tetra-t-butyl-p-sexiphenyl; 3,5,3″″,5″″-tetra-t-butyl-p-quinquephenyl; 2,3,5,6-1H,4H-tetrahydro-9-acetylquinolizino-<9,9a,1-gh>coumarin; 2,3,5,6-1H,4H-tetrahydro-9-carboethoxyquinolizino-<9,9a,1-gh>coumarin; 2,3,5,6-1H,4H-tetrahydro-8-methylquinolizino-<9,9a,1-gh>coumarin; 2,3,5,6-1H,4H-tetrahydro-9-(3-pyridyl)-quinolizino-<9,9a,1-gh>coumarin; 2,3,5,6-1H,4H-tetrahydro-8-trifluoromethylquinolizino-<9,9a,1-gh>coumarin; 2,3,5,6-1H,4H-tetrahydroquinolizino-<9,9a,1-gh>coumarin; 3,3′,2″,3′″-tetramethyl-p-quaterphenyl; 2,5,2″″,5′″-tetramethyl-p-quinquephenyl; P-terphenyl; P-quaterphenyl; nile red; rhodamine 700; oxazine 750; rhodamine 800; IR 125; IR 144; IR 140; IR 132; IR 26; IRS; diphenylhexatriene; diphenylbutadiene; tetraphenylbutadiene; naphthalene; anthracene; 9,10-diphenylanthracene; pyrene; chrysene; rubrene; coronene; phenanthrene or the like, 3-hydroxyflavones such as disclosed in US 2009/0054586 A1, or combinations comprising at least one of the foregoing dyes.

The thermoplastic compositions can be manufactured by various methods. For example, powdered polycarbonate, impact modifier, epoxy additive, phenolic diphosphite, and/or other optional components can be first blended in a HENSCHEL-Mixer™ high speed mixer. Other low shear processes, including but not limited to hand mixing, can also accomplish this blending. The blend is then fed into the throat of a twin-screw extruder via a hopper. Alternatively, at least one of the components can be incorporated into the composition by feeding directly into the extruder at the throat and/or downstream through a sidestuffer. Additives can also be compounded into a masterbatch with a desired polymeric resin and fed into the extruder. The extruder is generally operated at a temperature higher than that necessary to cause the composition to flow. The extrudate is immediately quenched in a water batch and pelletized. The pellets, so prepared, when cutting the extrudate can be one-fourth inch long or less as desired. Such pellets can be used for subsequent molding, shaping, or forming.

The thermoplastic compositions are further illustrated by the following non-limiting examples.

EXAMPLES

The following components are used in the examples. PC1 was prepared using a bisphenol having sulfur content less than 2 ppm by weight and less than 150 ppm hydroxyl content, according to US2013/0035441A1 and US2013/0108820 A1. Unless specifically indicated otherwise, the amount of each component is in weight percent in the following examples, based on the total weight of the composition.

TABLE 1 Acronym Component Source PC1 BPA polycarbonate, MW about 30,000, SABIC CAS: 25971-63-5 PC2 BPA polycarbonate, MW about 30,000 SABIC CAS: 25971-63-5 I-168 Irgaphos ™ 168, CIBA tris(2,4-di-t-butylphenyl) phosphite CAS: 31570-04-4 D S-9228 Doverphos ™ S-9228, Dover bis(2,4-dicumyl) pentaerythritol Chemical diphosphite CAS: 154862-43-8 PEP 36 ADK stab PEP 36, Bis(tri-alkylated ADEKA phenyl)-PEDP CAS: 80693-00-1 PALMAROLE TPP Triphenylphosphine BASF CAS: 603-35-0 A 1076 Antioxidant 1076, CHEMTURA Octadecyl 3-(3,5-di-tert-butyl-4- hydroxyphenyl)propionate, CAS: 2082-79-3 CA Epoxy Cycloaliphatic Epoxy Resin, IMCDgroup 3,4-epoxycyclohexylmethyl-3,4- epoxycyclohexyl carboxylate CAS: 2386-87-0 Epoxydized Epoxidized Soyabean Oil Sigma Aldrich SB oil CAS: 8013-07-8 DER 671 DER 671 Epoxy Resin, Hexion Epoxy Bisphenol A-(epichlorohydrin); Specialty epoxy resin (avg: Mw 700-1100) Chemicals CAS: 25068-38-6

All thermoplastic compositions except where indicated are compounded on an intermeshing co-rotating twin-screw extruder to form pellets of the composition, using a temperature of 280° C. to 300° C. and a heating residence time of about 30 seconds. The compositions are subsequently molded using an ENGEL 75T injection molder with AXXICON insert mold system to mold 60 mm×60 mm×2.5 mm color test plaques at standard molding conditions with a temperature of about 290° C. and a residence time about 5 minutes.

The plaques are first measured for color on a Macbeth 7000A spectrophotometer in transmission mode and UV excluded. CIELAB 1976 color values (L*, a*, b*) (ISO 11664-4:2008(E)/CIE S 014-4/E:2007 are determined from the absorption spectrum of a 2.5 mm thick color plaque between 400 nm and 700 nm. Yellowness index (YI) values can be calculated according to ASTM D1925-E313. The plaques can also be measured for transmission and haze according to ASTM D1003-00 using a BYK Gardner Haze-gard dual. After initial color measurements, the plaques are subjected to aging in a circulating air oven at 130° C. for up to 2000 hours. Periodically (after aging for 50 hours, 250 hours, 500 hours, 750 hours, 1000 hours, and 2000 hours), the samples are removed from the oven, measured for color as described above, and returned to the oven. The change in color after aging, expressed as dE (2000 hrs.).

Examples 1-4 and Comparative Examples 1-10

Plaques were prepared from thermoplastic compositions as set forth in Tables 2, 3 and 4 and subjected to aging with color measurements as described above. CIELAB 1976 L*, a*, and b* values, along with dE (2000 hrs.) values based on a comparison of initial color measurements and color measurements taken after 2000 hours of aging at 130° C., are shown in Tables 2, 3 and 4 according to ISO 11664-4:2008(E)/CIE S 014-4/E:2007 using CIE illuminant D65 and a 2.5 mm thick molded plaque of the thermoplastic composition.

TABLE 2 PC1 PC2 1-168 D S-9228 sample (% wt) (% wt) (% wt) (% wt) PEP 36 (% wt) TPP (% wt) A 1076 (% wt) L* a* b* dE (2000 hrs.) CE1 100 95.83 −0.08 0.80 1.70 CE2 100 95.54 −0.18 1.47 5.86 CE3 99.95 0.05 95.83 −0.08 0.63 2.38 CE4 99.9 0.1 95.90 −0.05 0.58 2.24 CE5 99.8 0.2 95.90 −0.04 0.54 6.21 CE6 99.95 0.05 95.84 −0.06 0.56 5.49 CE7 99.9 0.1 95.87 −0.05 0.51 7.49 CE8 99.8 0.2 95.90 −0.03 0.49 52.54 CE9 99.95 0.05 95.88 −0.05 0.52 4.03 CE10 99.9 0.1 95.90 −0.03 0.52 30.28 CE11 99.8 0.2 95.94 −0.03 0.45 70.75 CE12 99.95 0.05 95.87 −0.06 0.53 3.34 CE13 99.9 0.1 95.92 −0.04 0.48 2.90 CE14 99.8 0.2 95.91 −0.06 0.54 4.01 CE15 99.9 0.1 95.76 −0.09 0.83 11.50 CE16 99.98 0.02 95.87 −0.07 0.63 1.09 CE17 99.96 0.04 95.85 −0.08 0.75 1.71 CE18 99.93 0.05 0.02 95.85 −0.06 0.57 0.99 CE42 99.97 0.01 0.02 95.85 −0.07 0.57 1.17 CE19 99.93 0.05 0.02 95.87 −0.06 0.54 1.41 CE20 99.88 0.1 0.02 95.90 −0.05 0.49 2.46 CE21 99.78 0.2 0.02 95.90 −0.06 0.49 24.93 CE22 99.93 0.05 0.02 95.92 −0.05 0.50 9.85 CE23 99.88 0.1 0.02 95.92 −0.05 0.49 36.54 CE24 99.93 0.05 0.02 95.91 −0.04 0.48 4.48 CE25 99.88 0.1 0.02 95.90 −0.04 0.48 5.75

TABLE 3 PC1 PC2 I-168 D S-9228 PEP 36 TPP A 1076 CA Epoxy dE sample (% wt) (% wt) (% wt) (% wt) (% wt) (% wt) (% wt) (% wt) L* a* b* (2000 hrs.) CE26 99.9 0.1 95.81 −0.08 0.80 2.59 CE27 99.95 0.05 95.84 −0.09 0.75 1.74 CE30 99.85 0.1 0.05 95.91 −0.05 0.56 1.67 CE31 99.7 0.2 0.1 95.90 −0.04 0.53 1.36 EX1 99.85 0.1 0.05 95.90 −0.04 0.50 1.93 EX2 99.7 0.2 0.1 95.90 −0.03 0.47 1.76 EX3 99.85 0.1 0.05 95.92 −0.04 0.52 1.88 CE32 99.7 0.2 0.1 95.93 −0.03 0.46 14.71 CE33 99.85 0.1 0.05 95.91 −0.10 0.63 2.54 CE34 99.7 0.2 0.1 95.88 −0.10 0.69 4.15 CE37 99.85 0.1 0.05 95.70 −0.11 0.95 9.78 CE38 99.93 0.02 0.05 95.85 −0.08 0.76 1.00 CE39 99.83 0.1 0.02 0.05 95.91 −0.05 0.57 0.78 EX7 99.92 0.01 0.02 0.05 95.88 −0.06 0.57 0.71 EX6 99.88 0.05 0.02 0.05 95.88 −0.04 0.52 0.79 EX4 99.83 0.1 0.02 0.05 95.90 −0.05 0.50 0.84 EX5 99.83 0.1 0.02 0.05 95.92 −0.04 0.49 1.81 CE40 99.83 0.1 0.02 0.05 95.90 −0.11 0.66 1.90

TABLE 4 sample PC1 (% wt) D S-9228 (% wt) Epoxydized SB oil (% wt) DER 671 Epoxy (% wt) L* a* b* dE (2000 hrs.) CE28 99.95 0.05 95.85 −0.09 0.76 1.66 CE29 99.95 0.05 95.83 −0.09 0.80 1.60 CE35 99.85 0.1 0.05 95.87 −0.05 0.61 2.33 CE36 99.85 0.1 0.05 95.89 −0.05 0.55 2.22

As shown in Table 2, phosphite stabilizers as well as triphenylphospine (CE3 to CE14) give better starting color (lower b*) after processing compared to polycarbonate without stabilizers (CE1). Pentaerithrol based phosphites are more effective in reducing color than the other stabilizers. All these P-containing stabilizers lead to worse color stability (higher delta E). This effect is again the strongest for pentaerithrol based phosphites. Table 2 also shows that PC1 leads to lower color and improved color stability than PC2. Table 2 also shows that for many polycarbonate compositions, such as those having a free hydroxy content of greater than 150 ppm and/or prepared from a bisphenol having a sulfur content of greater than 2 ppm by weight, the epoxy additive can actually increase the yellowness of molded articles. See, e.g., a comparison of CE15 and CE37 in Tables 2 and 3.

The addition of Antioxidant 1076 has a positive effect on color stability, as shown by examples CE16 to CE25, but in combination with higher levels of pentaerithrol based stabilizers, discoloration remains higher than the target value of 2.0. In combination with another phosphite stabilizer such as 1-168, color stability is good, but initial color is too yellow (CE16, CE17) b*>0.56.

The use of epoxide typically does not lead to improved color stability as shown by the samples in Tables 2 and 3. Comparing CE26 and CE27 with CE1, it is shown that higher levels of epoxy reduce color stability. Surprisingly however, it was found that the epoxide can improve color stability when it is used in combination with phosphites, in particular those based on pentaerithrol such as Doverphos S-9228 and ADK STB PEP-36. This is illustrated by comparing EX1 and EX2 with CE7 and CE8, comparing EX3 and CE32 with CE10 and CE11 and by comparing EX4 and EX5 with CE20 and CE23. The comparison is shown graphically in FIGS. 3 and 4, which plot dE as a function of the D S-9882 phosphite for compositions with and without epoxide. The plots show a sharp increase in dE (2000 hrs.) when Doverphos level exceeds 0.1 wt. % for the composition without an epoxide, but stable dE (2000 hrs.) at Doverphos levels over 0.1 wt. % for the composition with the epoxide additive.

Table 4 shows that not all epoxy containing materials are effective. Epoxydized soybean oil and DER 671 epoxy do not result in color stability improvement.

Set forth below are some embodiments of the illuminating device and methods of making and using the same.

Embodiment 1: An illuminating device, comprising: a light source; and a light-transmitting article formed from a thermoplastic composition, positioned to provide a light transmission path from the light source through the light-transmitting article, with a distance, d, between the light source and the light-transmitting article of less than 40 mm, the light transmission path extending through the light-transmitting article and optionally through other light-transmitting article(s) comprising the thermoplastic composition such that the total distance, p, of the light transmission path through the light-transmitting article is at least 3 mm; wherein the thermoplastic composition comprises a polycarbonate having repeating structural carbonate units according to the formula

in which at least 60 percent of the total number of R¹ groups contain aromatic moieties and the balance thereof are aliphatic, alicyclic, or aromatic; the polycarbonate having been prepared through an interfacial polymerization process from BPA monomer having an organic purity higher than 99.70% by weight and having a hydroxyl content lower than 150 ppm by weight; 0.01 wt. % to 0.30 wt. %, based on the total weight of the thermoplastic composition, of an epoxy additive having at least two epoxy groups per molecule; and 0.01 wt. % to 0.30 wt. %, based on the total weight of the thermoplastic composition, of a phenolic diphosphite derived from pentaerythritol; wherein the thermoplastic composition has a sulfur content lower than 2 ppm, and wherein the thermoplastic composition exhibits a dE (2000 hrs.) value of less than 2.0 after 2000 hours of heat aging at 130° C., measured according ISO 11664-4:2008(E)/CIE S 014-4/E:2007 using CIE illuminant D65 and a 2.5 mm thick molded plaque of the thermoplastic composition.

Embodiment 2: The illuminating device of Embodiment 1, wherein p is at least 5 mm.

Embodiment 3: The illuminating device of Embodiment 1, wherein p is at least 10 mm.

Embodiment 4: The illuminating device of Embodiment 1, wherein p is at least 20 mm.

Embodiment 5: The illuminating device of any of Embodiments 1-4, wherein d is less than 20 mm.

Embodiment 6: The illuminating device of any of Embodiments 1-4, wherein d is less than 10 mm.

Embodiment 7: The illuminating device of any of Embodiments 1-4, wherein d is less than 5 mm.

Embodiment 8: The illuminating device of any of Embodiments 1-4, wherein d is 0.

Embodiment 9: The illuminating device of any of Embodiments 1-8, wherein the thermoplastic composition exhibits the dE value of less than 1.50 after 2000 hours of heat aging at 130° C., measured according ISO 11664-4:2008(E)/CIE S 014-4/E:2007 using CIE illuminant D65 and a 2.5 mm thick molded plaque of the thermoplastic composition.

Embodiment 10: The illuminating device of any of Embodiments 1-8, wherein the thermoplastic composition exhibits the dE value of less than 0.95 after 2000 hours of heat aging at 130° C., measured according ISO 11664-4:2008(E)/CIE S 014-4/E:2007 using CIE illuminant D65 and a 2.5 mm thick molded plaque of the thermoplastic composition.

Embodiment 11: The illuminating device of any of Embodiments 1-10, wherein the thermoplastic composition exhibits a b*<0.56 and a L*>95.65 as measured according ISO 11664-4:2008(E)/CIE S 014-4/E:2007 using CIE illuminant D65 and a 2.5 mm thick molded plaque of the thermoplastic composition.

Embodiment 12: The illuminating device of any of Embodiments 1-10, wherein the thermoplastic composition exhibits a b* of <0.54 and a L*>95.75 as measured according ISO 11664-4:2008(E)/CIE S 014-4/E:2007 using CIE illuminant D65 and a 2.5 mm thick molded plaque of the thermoplastic composition.

Embodiment 13: The illuminating device of any of Embodiments 1-10, wherein the thermoplastic composition exhibits a b* of <0.52 and a L*>98.85 as measured according ISO 11664-4:2008(E)/CIE S 014-4/E:2007 using CIE illuminant D65 and a 2.5 mm thick molded plaque of the thermoplastic composition.

Embodiment 14: The illuminating device of any of Embodiments 1-13, wherein the epoxy additive is an aliphatic epoxide having at least two epoxy groups per molecule and a molecular weight less than 600 g/mol.

Embodiment 15: The illuminating device of any of Embodiments 1-13, wherein the epoxy additive is a carboxylate epoxy resin.

Embodiment 16: The illuminating device of Embodiment 15, wherein the epoxy additive is a carboxylate epoxy resin comprising a carboxylate diepoxide according to the formula:

Embodiment 17: The illuminating device of any of Embodiments 1-16, wherein the phenolic diphosphite is according to the formula:

wherein R₁, R₂, R₃, R₄, R₅, R₆, R₇, R₈, R₉, and R₁₀ each independently represents hydrogen or a C₁₋₂₀ organic radical.

Embodiment 18: The illuminating device of Embodiment 17, wherein R₂, R₅, R₅, R₇, R₉, and R₁₀ are H and R₁, R₂, R₆, and R₈ each independently represents a C₁₋₂₀ organic radical.

Embodiment 19: The illuminating device of Embodiment 18, wherein R₁, R₃, R₆, and R₈ each independently represents an alkaryl radical of 4 to 13 carbon atoms.

Embodiment 20: The illuminating device of Embodiment 19, wherein R₁, R₃, R₆, and R₈ are each cumyl.

Embodiment 21: The illuminating device of Embodiment 17 wherein at least 40% of the R₁, R₂, R₃, R₄, R₅, R₆, R₇, R₈, R₉, and R₁₀ groups are cumyl.

Embodiment 22: The illuminating device of any of Embodiments 1-16, wherein at least 90% of the R¹ groups are derived from the bisphenol.

Embodiment 23: The illuminating device of Embodiment 22, wherein all of the R¹ groups are derived from the bisphenol.

Embodiment 24: The illuminating device of any of Embodiments 1-23, wherein the bisphenol is bisphenol A.

Embodiment 25: The illuminating device of Embodiments 1-24, wherein the thermoplastic composition comprises from 0.02 wt. % to 0.10 wt. % of the epoxy additive.

Embodiment 26: The illuminating device of Embodiments 1-25 wherein the thermoplastic composition comprises from 0.05 wt. % to 0.20 wt. % of the phenolic diphosphite.

Embodiment 27: The illuminating device of any of Embodiments 1-26, wherein the light-transmitting article is an illuminant lens, illuminant cover, a light guide, or an optical sheet.

Embodiment 28: The illuminating device of any of Embodiments 27, wherein the light-transmitting article comprises a light guide wherein p is at least 7 mm.

Embodiment 29: The illuminating device of any of Embodiments 1-28, wherein the illuminating device is a display object, a toy, furniture, an art object, or a light.

Embodiment 30: The illuminating device of Embodiment 29, wherein the illuminating device is a motor vehicle headlamp.

Embodiment 31: The illuminating device of any of Embodiments 1-30, wherein the light-transmitting article comprises an aspheric lens.

Embodiment 32: The illuminating device of any of Embodiments 1-31, wherein the light-transmitting article is a first lens along said light transmission path, and further comprising a second lens along said light transmission path further from the light source than the first lens, said second lens comprises the thermoplastic composition.

Embodiment 33: The illuminating device of any of Embodiments 1-32, wherein the light source is a light-emitting diode.

Embodiment 34: The illuminating device of any of Embodiments 1-32, wherein the light source is a xenon arc lamp.

Embodiment 35: The illuminating device of any of Embodiments 1-34, wherein the light-transmitting article reaches a temperature between 80° C. and 135° C. during operation.

Embodiment 36: The illuminating device of any of Embodiments 1-34, wherein the sulfur content is greater than 0 to less than 2 ppm.

Embodiment 37: The illuminating device of Embodiment 36, wherein the sulfur content is 0.5 ppm to less than 2 ppm.

Embodiment 38: The illuminating device of Embodiment 36, wherein the sulfur content is less than 0.5 ppm.

Embodiment 39: A method of using the device of any of Embodiments 1-38, comprising illuminating the light-transmitting article with the light source under conditions to subject the light-transmitting article to a temperature of 80° C. to 135° C.

Embodiment 40: The method of Embodiment 39, wherein the light-transmitting article is subjected to a temperature 80° C. to 135° C. for a cumulative duration of at least 500 hours.

Embodiment 41: A method for making the illuminating device of any of Embodiments 1-38, comprising: disposing the light source the distance d of less than 40 mm from the light-transmitting plastic article such that the total distance, p, of the light transmission path is at least 3 mm.

The singular forms “a,” “an,” and “the” include plural referents unless the context clearly dictates otherwise. “Or” means “and/or.” The modifier “about” used in connection with a quantity is inclusive of the stated value and has the meaning dictated by the context (e.g., includes the degree of error associated with measurement of the particular quantity). The notation “±10%” means that the indicated measurement can be from an amount that is minus 10% to an amount that is plus 10% of the stated value. The terms “front”, “back”, “bottom”, and/or “top” are used herein, unless otherwise noted, merely for convenience of description, and are not limited to any one position or spatial orientation. The endpoints of all ranges directed to the same component or property are inclusive and independently combinable (e.g., ranges of “less than or equal to 25 wt %, or 5 wt % to 20 wt %,” is inclusive of the endpoints and all intermediate values of the ranges of “5 wt % to 25 wt %,” etc.). The suffix “(s)” is intended to include both the singular and the plural of the term that it modifies, thereby including at least one of that term (e.g., ‘the colorant(s)’ includes a single colorant or two or more colorants, i.e., at least one colorant). “Optional” or “optionally” means that the subsequently described event or circumstance can or cannot occur, and that the description includes instances where the event occurs and instances where it does not. A “combination” is inclusive of blends, mixtures, alloys, reaction products, and the like. Unless otherwise specified, all optical parameters herein are measured on 2.5 mm thick plaques. Unless otherwise specified, parts per million (ppm) is by weight.

As used herein, the term “hydrocarbyl” and “hydrocarbon” refers broadly to a substituent comprising carbon and hydrogen, optionally with 1 to 3 heteroatoms, for example, oxygen, nitrogen, halogen, silicon, sulfur, or a combination thereof; “alkyl” refers to a straight or branched chain, saturated monovalent hydrocarbon group; “alkylene” refers to a straight or branched chain, saturated, divalent hydrocarbon group; “alkylidene” refers to a straight or branched chain, saturated divalent hydrocarbon group, with both valences on a single common carbon atom; “alkenyl” refers to a straight or branched chain monovalent hydrocarbon group having at least two carbons joined by a carbon-carbon double bond; “cycloalkyl” refers to a non-aromatic monovalent monocyclic or multicyclic hydrocarbon group having at least three carbon atoms, “cycloalkenyl” refers to a non-aromatic cyclic divalent hydrocarbon group having at least three carbon atoms, with at least one degree of unsaturation; “aryl” refers to an aromatic monovalent group containing only carbon in the aromatic ring or rings; “arylene” refers to an aromatic divalent group containing only carbon in the aromatic ring or rings; “alkylaryl” refers to an aryl group that has been substituted with an alkyl group as defined above, with 4-methylphenyl being an exemplary alkylaryl group; “arylalkyl” refers to an alkyl group that has been substituted with an aryl group as defined above, with benzyl being an exemplary arylalkyl group; “acyl” refers to an alkyl group as defined above with the indicated number of carbon atoms attached through a carbonyl carbon bridge (—C(═O)—); “alkoxy” refers to an alkyl group as defined above with the indicated number of carbon atoms attached through an oxygen bridge (—O—); and “aryloxy” refers to an aryl group as defined above with the indicated number of carbon atoms attached through an oxygen bridge (—O—).

Unless otherwise indicated, each of the foregoing groups can be unsubstituted or substituted, provided that the substitution does not significantly adversely affect synthesis, stability, or use of the compound. The term “substituted” as used herein means that at least one hydrogen on the designated atom or group is replaced with another group, provided that the designated atom's normal valence is not exceeded. When the substituent is oxo (i.e., ═O), then two hydrogens on the atom are replaced. Combinations of substituents and/or variables are permissible provided that the substitutions do not significantly adversely affect synthesis or use of the compound. Exemplary groups that can be present on a “substituted” position include, but are not limited to, cyano; hydroxyl; nitro; azido; alkanoyl (such as a C2-6 alkanoyl group such as acyl); carboxamido; C1-6 or C1-3 alkyl, cycloalkyl, alkenyl, and alkynyl (including groups having at least one unsaturated linkages and from 2 to 8, or 2 to 6 carbon atoms); C1-6 or C1-3 alkoxy groups; C6-10 aryloxy such as phenoxy; C1-6 alkylthio; C1-6 or C1-3 alkylsulfinyl; C1-6 or C1-3 alkylsulfonyl; aminodi(C1-6 or C1-3)alkyl; C6-12 aryl having at least one aromatic rings (e.g., phenyl, biphenyl, naphthyl, or the like, each ring either substituted or unsubstituted aromatic); C7-19 alkylenearyl having 1 to 3 separate or fused rings and from 6 to 18 ring carbon atoms, with benzyl being an exemplary arylalkyl group; or arylalkoxy having 1 to 3 separate or fused rings and from 6 to 18 ring carbon atoms, with benzyloxy being an exemplary arylalkoxy group.

All cited patents, patent applications, and other references are incorporated herein by reference in thaeir entirety. However, if a term in the present application contradicts or conflicts with a term in the incorporated reference, the term from the present application takes precedence over the conflicting term from the incorporated reference.

While typical embodiments have been set forth for the purpose of illustration, the foregoing descriptions should not be deemed to be a limitation on the scope herein. Accordingly, various modifications, adaptations, and alternatives can occur to one skilled in the art without departing from the spirit and scope herein. 

What is claimed is:
 1. An illuminating device, comprising: a light source; and a light-transmitting article formed from a thermoplastic composition, positioned to provide a light transmission path from the light source through the light-transmitting article, with a distance, d, between the light source and the light-transmitting article of less than 40 mm, the light transmission path extending through the light-transmitting article and optionally through other light-transmitting article(s) comprising the thermoplastic composition such that the total distance, p, of the light transmission path through the light-transmitting article is at least 3 mm; wherein the thermoplastic composition comprises a polycarbonate; the polycarbonate having been prepared through an interfacial polymerization process from BPA monomer having an organic purity higher than 99.70% by weight and having a hydroxyl content lower than 150 ppm by weight; 0.01 wt. % to 0.30 wt. %, based on the total weight of the thermoplastic composition, of an epoxy additive having at least two epoxy groups per molecule; and 0.01 wt. % to 0.30 wt. %, based on the total weight of the thermoplastic composition, of a phenolic diphosphite obtained from pentaerythritol; wherein the thermoplastic composition has a sulfur content lower than 2 ppm; and wherein the thermoplastic composition exhibits a dE (2000hrs.) value of less than 2.0 after 2000 hours of heat aging at 130° C., measured according ISO 11664-4:2008(E)/CIE S 014-4/E:2007 using CIE illuminant D65 and a 2.5 mm thick molded plaque of the thermoplastic composition.
 2. The illuminating device of claim 1, wherein p is at least 5 mm.
 3. The illuminating device of claim 1, wherein d is less than 20 mm.
 4. The illuminating device of claim 1, wherein d is less than 5 mm.
 5. The illuminating device of claim 1, wherein the thermoplastic composition exhibits the dE value of less than 1.50 after 2000 hours of heat aging at 130° C., measured according ISO 11664-4:2008(E)/CIE S 014-4/E:2007 using CIE illuminant D65 and a 2.5 mm thick molded plaque of the thermoplastic composition.
 6. The illuminating device of claim 1, wherein the thermoplastic composition exhibits a b* <0.56 and a L* >95.65 as measured according ISO 11664-4:2008(E)/CIE S 014-4/E:2007 using CIE illuminant D65 and a 2.5 mm thick molded plaque of the thermoplastic composition.
 7. The illuminating device of claim 1, wherein the epoxy additive is an aliphatic epoxide having at least two epoxy groups per molecule and a molecular weight less than 600 g/mol.
 8. The illuminating device of claim 1, wherein the epoxy additive is a carboxylate epoxy resin.
 9. The illuminating device of claim 8, wherein the epoxy additive is a carboxylate epoxy resin comprising a carboxylate diepoxide according to the formula:


10. The illuminating device of claim 1, wherein the phenolic diphosphite is according to the formula:

wherein R₁, R₂, R₃, R₄, R₅, R₆, R₇, R₈, R₉, and R₁₀ each independently represents hydrogen or a C₁₋₂₀ organic radical.
 11. The illuminating device of claim 10, wherein R₂, R₅, R₅, R₇, R₉, and R₁₀ are H and R₁, R₂, R₆, and R₈ each independently represents a C₁₋₂₀organic radical.
 12. The illuminating device of claim 10 wherein at least 40% of the R₁, R₂, R₃, R₄, R₅, R₆, R₇, R₈, R₉, and R₁₀ groups are cumyl.
 13. The illuminating device of claim 1, wherein at least 90% of the R¹ groups are obtained from the bisphenol.
 14. The illuminating device of claim 13, wherein all of the R¹ groups are obtained from the bisphenol A.
 15. The illuminating device of claim 1, wherein the thermoplastic composition comprises from 0.02 wt. % to 0.10 wt. % of the epoxy additive.
 16. The illuminating device of claim 1, wherein the light-transmitting article is an illuminant lens, illuminant cover, a light guide, or an optical sheet.
 17. The illuminating device of claim 16, wherein the light-transmitting article comprises a light guide wherein p is at least 7 mm.
 18. The illuminating device of claim 1, wherein the illuminating device is a display object, a toy, furniture, an art object, or a light.
 19. The illuminating device of claim 18, wherein the illuminating device is a motor vehicle headlamp.
 20. The illuminating device of claim 1, wherein the light-transmitting article comprises an aspheric lens.
 21. The illuminating device of claim 1, wherein the light-transmitting article is a first lens along said light transmission path, and further comprising a second lens along said light transmission path further from the light source than the first lens, said second lens comprises the thermoplastic composition.
 22. The illuminating device of claim 1, wherein the light source is a light-emitting diode.
 23. The illuminating device of claim 1, wherein the light source is a xenon arc lamp.
 24. The illuminating device of claim 1, wherein the light-transmitting article reaches a temperature between 80° C. and 135° C. during operation. 